ERCC6 Chromosome 10
ERCC excision repair 6, chromatin remodeling factor
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What This Gene Does
This gene encodes a DNA-binding protein that is important in transcription-coupled excision repair. The encoded protein has ATP-stimulated ATPase activity, interacts with several transcription and excision repair proteins, and may promote complex formation at DNA repair sites. Mutations in this gene are associated with Cockayne syndrome type B and cerebrooculofacioskeletal syndrome 1. Alternative splicing occurs between a splice site from exon 5 of this gene to the 3' splice site upstream of the open reading frame (ORF) of the adjacent gene, piggyback-derived-3 (GeneID:267004), which activates the alternative polyadenylation site downstream of the piggyback-derived-3 ORF. The resulting transcripts encode a fusion protein that shares sequence with the product of each individual gene. [provided by RefSeq, Mar 2016]
Gene Info
Gene Group
"SNF2 related family|ERCC excision repair associated|B-WICH chromatin-remodelling complex subunits"
Locus Type
gene with protein product
Location
10q11.23
Ensembl
ENSG00000225830
Associated Conditions (28)
Cockayne syndrome
Cerebrooculofacioskeletal syndrome 1
ERCC6-related disorder
Age related macular degeneration 5
Cockayne syndrome type 2
Inborn genetic diseases
Thymoma
DE SANCTIS-CACCHIONE SYNDROME
Hereditary breast ovarian cancer syndrome
7 conditions
Cone-rod dystrophy
Intellectual disability
6 conditions
Clear cell carcinoma of kidney
Uveal melanoma
Colon adenocarcinoma
Melanoma
Malignant tumor of esophagus
Familial cancer of breast
Ovarian serous cystadenocarcinoma
+8 more conditions
Key Variants
RS1057518910
Conflicting classifications of pathogenicity
Cockayne syndrome, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome
Health Risk
RS114234514
Conflicting classifications of pathogenicity
ERCC6-related disorder, ERCC6-related disorder
Health Risk
RS114403790
Conflicting classifications of pathogenicity
Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2
Health Risk
RS114490473
Conflicting classifications of pathogenicity
Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
Health Risk
RS114832108
Conflicting classifications of pathogenicity
Health Risk
RS115633798
Conflicting classifications of pathogenicity
Inborn genetic diseases, Thymoma, Inborn genetic diseases
Health Risk
RS115643329
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS115875661
Conflicting classifications of pathogenicity
Health Risk
RS115876786
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS116032070
Conflicting classifications of pathogenicity
Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
Health Risk
RS1163269726
Conflicting classifications of pathogenicity
Inborn genetic diseases, Cockayne syndrome type 2, Inborn genetic diseases
Health Risk
RS117555054
Conflicting classifications of pathogenicity
Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2
Health Risk
All Variants (413)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS1057518910 | Health Risk | Conflicting classifications of pathogenicity | Cockayne syndrome, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome |
| RS114234514 | Health Risk | Conflicting classifications of pathogenicity | ERCC6-related disorder, ERCC6-related disorder |
| RS114403790 | Health Risk | Conflicting classifications of pathogenicity | Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2 |
| RS114490473 | Health Risk | Conflicting classifications of pathogenicity | Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2 |
| RS114832108 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS115633798 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Thymoma, Inborn genetic diseases |
| RS115643329 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS115875661 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS115876786 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS116032070 | Health Risk | Conflicting classifications of pathogenicity | Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2 |
| RS1163269726 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Cockayne syndrome type 2, Inborn genetic diseases |
| RS117555054 | Health Risk | Conflicting classifications of pathogenicity | Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2 |
| RS1275257135 | Health Risk | Conflicting classifications of pathogenicity | Cockayne syndrome type 2, Cockayne syndrome type 2 |
| RS1317145066 | Health Risk | Conflicting classifications of pathogenicity | Cerebrooculofacioskeletal syndrome 1, DE SANCTIS-CACCHIONE SYNDROME, Cockayne syndrome type 2 |
| RS1349103905 | Health Risk | Conflicting classifications of pathogenicity | Cockayne syndrome type 2, Cockayne syndrome type 2 |
| RS138756386 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS138758064 | Health Risk | Conflicting classifications of pathogenicity | Hereditary breast ovarian cancer syndrome, Hereditary breast ovarian cancer syndrome |
| RS138865542 | Health Risk | Conflicting classifications of pathogenicity | Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5 |
| RS139007661 | Health Risk | Conflicting classifications of pathogenicity | 7 conditions, DE SANCTIS-CACCHIONE SYNDROME, Inborn genetic diseases |
| RS139188695 | Health Risk | Conflicting classifications of pathogenicity | Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5 |
| RS141121035 | Health Risk | Conflicting classifications of pathogenicity | Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2 |
| RS141391984 | Health Risk | Conflicting classifications of pathogenicity | Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2 |
| RS142097249 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS1421008948 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS142219494 | Health Risk | Conflicting classifications of pathogenicity | ERCC6-related disorder, ERCC6-related disorder |
| RS142580756 | Health Risk | Conflicting classifications of pathogenicity | Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5 |
| RS142641602 | Health Risk | Conflicting classifications of pathogenicity | Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2 |
| RS143260457 | Health Risk | Conflicting classifications of pathogenicity | Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5 |
| RS144608959 | Health Risk | Conflicting classifications of pathogenicity | Age related macular degeneration 5, Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1 |
| RS145554525 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS145720191 | Health Risk | Conflicting classifications of pathogenicity | ERCC6-related disorder, Clear cell carcinoma of kidney, Uveal melanoma |
| RS146043988 | Health Risk | Conflicting classifications of pathogenicity | Age related macular degeneration 5, Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1 |
| RS146165518 | Health Risk | Conflicting classifications of pathogenicity | Cockayne syndrome type 2, Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1 |
| RS146690522 | Health Risk | Conflicting classifications of pathogenicity | Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5 |
| RS147079519 | Health Risk | Conflicting classifications of pathogenicity | Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2 |
| RS147637331 | Health Risk | Conflicting classifications of pathogenicity | Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2 |
| RS148095899 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS148295935 | Health Risk | Conflicting classifications of pathogenicity | Cockayne syndrome type 2, Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5 |
| RS148475034 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS148845653 | Health Risk | Conflicting classifications of pathogenicity | Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5 |
| RS149382642 | Health Risk | Conflicting classifications of pathogenicity | Cockayne syndrome type 2, Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1 |
| RS150065567 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS150277901 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS150762517 | Health Risk | Conflicting classifications of pathogenicity | Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2 |
| RS150935953 | Health Risk | Conflicting classifications of pathogenicity | Cerebrooculofacioskeletal syndrome 1, Age related macular degeneration 5, Cockayne syndrome type 2 |
| RS1590405627 | Health Risk | Conflicting classifications of pathogenicity | Cockayne syndrome, Cockayne syndrome |
| RS181327678 | Health Risk | Conflicting classifications of pathogenicity | Age related macular degeneration 5, Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2 |
| RS1837452924 | Health Risk | Conflicting classifications of pathogenicity | Cerebrooculofacioskeletal syndrome 1, Cockayne syndrome type 2, Age related macular degeneration 5 |
| RS1850797114 | Health Risk | Conflicting classifications of pathogenicity | 7 conditions, Magnetic resonance imaging of brain abnormal, Intellectual disability |
| RS186482480 | Health Risk | Conflicting classifications of pathogenicity | DE SANCTIS-CACCHIONE SYNDROME, ERCC6-related disorder, DE SANCTIS-CACCHIONE SYNDROME |